MLS quiz cards Flashcards

1
Q

Which of the following microcytic anemias has no relationship with iron metabolism?

  • Iron deficiency anemia

*Sideroblastic anemia

*Anemia of chronic inflammation

*Thalassemia

A

Thalassemia is the correct answer.

*Thalassemia is a condition in which hemoglobin amino chains are reduced or deleted & has no direct relationship with iron metabolism.

*iron deficiency is a direct result of not having iron available for hemoglobin formation.

  • Sideroblastic anemia results when iron is available but cannot be used for hemoglobin formation.

*Anemia of chronic inflammation occurs when iron is available in storage but cannot be released for use.

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2
Q

In what form must iron be when bound to hemoglobin for effective oxygen delivery?

  • Ferrous ion

*Ferric ion

*Ferritin

*Transferrin

A

Ferrous ion is the correct answer

*Iron must be in the 2+ state (ferrous) to be able to bind & effectively deliver oxygen to the tissue.

*Iron in the 3+ state (ferric) is able to bind oxygen but does not release it effectively to the tissue.

*Ferritin is a form of storage iron & is not found in the erythrocyte.

  • Transferrin is a transfer protein that delivers circulating iron to the tissues for storage or to developing erythrocytes for use.
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3
Q

The most common cause of iron deficiency worldwide is?

  • Nutritional deficiency

*Chronic GI bleed

*Malabsorption

*Gastric bypass surgery

A

The correct answer is Malabsorption

*The most common cause of IDA worldwide is malabsorption, especially among women and children.

  • Chronic GI bleeds, malabsorption syndromes, & gastric bypass surgery can all result in iron deficiency but are not as common as malabsorption.
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4
Q

You are analyzing a PCR run and see that one of your samples is a high positive but the internal control failed. What should you do?

*Result the sample as positive

*Result the sample as negative

*Result the sample as indeterminate

*Repeat the sample

A

This sample can be resulted as positive. The purpose of an internal control is to show amplification occurred. Internal controls add extra assurance to negative samples that they are true negatives. However, because this sample is positive, we know amplification occurred even without the internal control.

*The sample is positive, even though the internal control didn’t show up, therefore you would not result this sample as negative.

*Indeterminate results often occur from a sample being very low level positive, where you can not accurately differentiate between positive & negative. In this case the sample is a clear positive.

*This sample would not need to be repeated & can be resulted as is.

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5
Q

Which of the following EBV viral loads is least likely to be seen in a healthy individual?

*Undetected viral load
* 35 IU/mL
*75 IU/mL
*7,500 IU/mL

A

EBV is a virus that commonly affects children & then lays dormant in the body, being able to be detected at low circulating viral loads in most healthy adults. There is no definitive threshold for a clinically relevant EBV viral load, but higher viral loads are less likely to be seen in healthy individuals.

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6
Q

Uric acid is the final breakdown product of what two purines?

*Adenine & Thymine

*Thymine & Cytosine

*Adenine & Guanine

*Guanine & Thymine

A

The purines adenine & guanine are broken down into uric acid.

Cytosine & thymine are pyrimidines that are mostly broken down into ammonia, carbon dioxide, and water but not into uric acid

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7
Q

A culture was performed on a stool sample. After growth was obtained on the blood agar plate, the gram stain showed curved gram-negative rods. the oxidase, catalase, and urease were positive. What is the most likely bacterial identification?

*Helicobacter pylori

*Campylobacter concisus

*Helicobacter cinaedi

*Arcobacter spp.

A

the correct answer is Helicobacter pylori. Identification methods for curved gram-negative rods will include (in this order) oxidase, catalase, and urease. Helicobacter pylori will have the gram stain showing curved gram -negative rods. It will have positive results for oxidase, catalase, & urease.

Campylobacter concisus will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase along with a negative catalase results.

Helicobacter cinaedi will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase & catalase along with a negative urease test.

Arcobacter spp. will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase & catalase along with a negative urease test.

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8
Q

How will unmethylated cytosine residues appear in a pyrogram after bisulfite treatment?

  • As cytosine
  • As uracil
  • As thymine
  • As guanine
A

Thymine is the correct answer.
bisulfite treatment converts unmethylated cytosine’s into uracil, which will then appear as thymine in the pyrogram, as the original DNA sequence would have thymine in it rather than uracil.

Any cytosine peaks in the pyrogram would be the results of methylated cytosine in the sequence.

A guanine peak would indicate a guanine nucleotide.

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9
Q

During DNA isolation, which of the following reagents is used to precipitate nucleic acids?

  • TEMED
    *Alcohols such as ethanol or isopropanol
    *DEPC water
    *Chloroform
A

Ethanol and Isopropanol are commonly used in molecular techniques for the precipitation of nucleic acids, DNA purification requires lysis of cells using NaOH & SDS; acidification using acetic acid and salt; extraction using phenol and chloroform; and lastly, precipitation of DNA which requires ethanol or isopropanol.

TEMED is tetramethylenediamine which is used as a catalyst for the solidification of polyacrylamide gels.

DEPC water is diethyl pyrocarbonate, a reagent that inactivates RNases.

Chloroform is used in the extraction step to solubilize DNA.

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10
Q

A stool specimen can be suspected of harboring Vibrio cholerae if it possesses which of the following characteristics?

  • if the stool is well formed and shows blood steaks.

*if the stool is soft, dark, & positive for occult blood.

*if the stool contains a high concentration of segmented neutrophils.

*if the stool is watery with a high pH and flecks of mucus.

A

Diarrhea caused by V. cholera is watery & contains large concentrations of Na, bicarbonate, & other electrolytes, producing an alkaline pH. The diarrhea is caused by the action of cholera toxin on the intestinal epithelial cells, with the end results of stimulating adenyl cyclase ( cyclic AMP), which in turn inhibits the reabsorption of Na across the brush border membrane & stimulates the excretion of bicarbonate & potassium into the bowel lumen. A stool specimen comprised of primarily fluid and flecks of mucous (known as rice water stools) is a distinctive feature when cholera toxin activity is present.

In the absence of mucosal invasion by the bacteria, blood or neutrophils are not found in the stool specimen.

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11
Q

Targeting the conserved regions of the 16s rRNA is commonly used to detect all, but which of the following organisms?

*Streptococcus
pneumoniae

*Chlamydia trachomatis

  • Mycobacterium tuberculosis
  • Mycoplasma hominis
A

Streptococcus pneumoniae is the correct answer.

Molecular methods for detecting Streptococcus pneumoniae target multiple genes, including penicillin-binding proteins & lysins. However, 16s rRNA is not typically used.

While the remaining three organisms may be detected through other gene targets, 16s rRNA is commonly used.

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12
Q

A sample has reactions occurring at immediate spin & AHG in a panel that showed varying reaction strengths. There is no obvious pattern that matches a particular panel cell or single antigen profile & the auto-control was negative. Which of the following is the most likely cause?

  • An IgM and an IgG antibody

*An IgG antibody only

*An IgM antibody

*An autoantibody

A

The cause would be the presence of both an IgM & an IgG antibody. Laboratorians should think of multiple antibodies when reactions are occurring at two different phases (IS and AHG), varying strengths in reactions, and no definite patterns. Patterns can sometimes be recognized if you look at each phase individually. For example reactions at IS may match an M antibody, & reactions at AHG may match a D antibody. Varying strengths in reaction could also indicate dosage occurring.

IgM antibodies most often react at IS, room temp, or colder.

IgG antibodies are most often detected at the AHG phase.

Since the autocontrol is negative, the positive reactions are caused by an alloantibody and not autoantibody.

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13
Q

Which of the following are markers currently used to differentiate heart failure from lung disease?

*TnI & TnT

*BNP & NT- proBNP

*Myoglobin & LD

*hs-CRP & homocysteine

A

BNP & NT-proBNP are currently used to differentiate Heart failure from lung disease.

TnI & TnT are currently used to diagnose acute coronary syndrome & acute myocardial infarction.

Myoglobin & LD are no longer used or are less commonly used as biomarkers for cardiac disease.

hs-CRP & homocysteine are used for cardiovascular risk stratification.

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14
Q

The type of hypersensitivity reaction associated with macrophage activation, cytokine-mediated inflammation is?

  • Type 1 Anaphylactic ( Immediate hypersensitivity)

*Type 2 Cytotoxic (Antibody mediated & antibody dependent, complement mediated hypersensitivity)

*Type 3 immune complex mediated hypersensitivity

*Type 4 cell mediated hypersensitivity (T-cell dependent).

A

Type 4 cell-mediated hypersensitivity is associated with macrophage activation. type 4 is characterized by direct target cell lysis & cytokine-mediated inflammation. There are 3 defining characteristics of type 4 hypersensitivity reactions: (1) Type 4 delayed-type hypersensitivity involving antigen-sensitized T cells or particles that remain phagocytized in a macrophage & are encountered by previously activated T cells for a second or subsequent time. Delayed hypersensitivity is a major defense mechanism again various intracellular pathogens, including mycobacteria, fungi, & certain parasites. (2) Rejection of foreign tissue grafts, elimination of tumor cells bearing neoantigens. (3) Formation of chronic granulomas.

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15
Q

What is the best method for lysing tough bacterial cell walls when the integrity of the chromosomal DNA is important?

*Enzyme digestion

*Bead beating

*Boiling

*Grinding

A

The correct answer is Enzyme digestion.
Enzymes can be formulated to be gentle enough to lyse cell walls without damaging chromosomal DNA.

Mechanical lysis, such as bead beating and grinding will effectively lyse cell walls but may also damage the DNA.

Boiling will also denature chromosomal DNA to a point where it may not be able to be renatured.

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16
Q

The laboratory test most commonly used to establish a definitive diagnosis of primary syphilis is:

*Rapid plasma reagin (RPR)

*recovery of spirochetes via culture.

*Direct fluorescent antibody test

*Fluorescent treponemal antibody (FTA) with absorption test.

A

Direct fluorescent antibody test is the definitive method for diagnosis early syphilis. The antibodies produced in response to infection with Treponema pallidum are detectable during primary syphilis. Levels will continue to increase as the disease progresses to secondary syphilis.

The RPR is a screening test. The test detects the presence of cardiolipin and other indicators that correlate to disease activity; however it isn’t highly specific and doesn’t correlate with disease activity.

Spirochetes cannot be recovered outside of the body and thus cannot be cultured.

FTA with absorption is done to diagnose late latent or tertiary syphilis.

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17
Q

What determines the fragment size generated in Sanger sequencing?

*Random incorporation of a ddNTP

*Incorporation of a ddNTP in a specific position

*Random incorporation of a dNTP

*Incorporation of a dNTP in a specific position

A

The correct answer is random incorporation of a ddNTP.

When chains are synthesized in Sanger sequencing, both dNTPs & ddNTPs are added to the master mix, which one gets added into the sequence is completely random. When a dNTP is added to the chain, it gets extended, but when a ddNTP is added, synthesis stops since ddNTPs lack the oxygen needed to bind the next nucleotide. The random incorporation of these ddNTPs leads to fragments of different lengths.

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18
Q

Which of the following organisms causes Q fever?

*Coxiella burnetii

*Anaplasma spp.

*Orientia tsutsugamushi

*Rickettsia rickettsii

A

Q fever, an acute systemic infection affecting the lungs, is caused by Coxiella burnetii.

Anaplasma spp. causes granulocytic anaplasmosis.

Orientia tsutsugamushi causes scrub typhus.

Rickettsia rickettsii causes Rocky Mountain spotted fever.

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19
Q

Which of the following laboratories DO NOT belong in the Clinical Pathology Laboratory?

  • Histology & Cytology

*Hematology & Coagulation

*Urinalysis & Flow Cytometry

*Immunology & Immunohematology

A

Histology & Cytology are part of the Anatomical & Surgical Pathology laboratories. Histology is the microscopic study of tissues. In this department, tissues are microscopically examined by pathologist to determine if they are normal or diseased. Cytology is the department where cells in the body tissues & fluids are counted, identified, & studied in order to determine if they are normal, malignant, or premalignant.

Hematology, Coagulation, Urinalysis, Flow Cytometry, Immunology, & Immunohematology, along with Microbiology & Clinical Chemistry, are departments of the Clinical Pathology Laboratories.

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20
Q

Donation of which apheresis blood product more than once every four weeks requires monitoring of total plasma protein & antibody levels?

*Red cell apheresis

*Platelepheresis

*Plasmapheresis

*Leukapheresis

A

Plasmapheresis is the correct answer. Plasma levels of total protein, IgG, & IgM must be monitored every four months in plasmapheresis donors because levels of these & other proteins present in plasma decrease following plasmapheresis.

Blood components from red cell apheresis, platletpheresis, & leukapheresis do not contain enough volume of plasma to necessitate the monitoring of plasma proteins.

21
Q

What modification is made to sample DNA during the bisulfite treatment step of bisulfite DNA sequencing?

*Methylated cytosine is deaminated & converted to uracil.

*Unmethylated cytosine is deaminated & converted to uracil.

*Methylated guanine is deaminated & converted to adenine.

*Unmethylated guanine is deaminated & converted to adenine.

A

The correct answer is Unmethylated cytosine is deaminated & converted to uracil. Bisulfite converts unmethylated cytosine to uracil by removing an amino group.

Methylated cytosine (5-methylcytosine) is unchanged by bisulfite because the methyl group prevents amine from being removed.

Guanine is not epigenetically modified by methylation, so there is no methylated guanine in patient samples.

Unmethylated guanine is not altered by bisulfite

22
Q

dTTP is replaced by dUTP-UNG system for what purpose?

*Contamination control

*If the starting template is RNA

*Required for RT-PCRs

*Required for nested PCRs

A

The correct answer is Contamination control. The dUTP-UNG system replaces dTTP with dUTP so that uracil-N-glycosylase (UNG) can be added before the next PCR to degrade any remnant amplicon that could potentially contaminate the next PCR. This is used as a contamination technique.
When RNA is used as the starting template, as is true in RT-PCRs, the DUTP-UNG systemcan be used, but isn’t necessary for the reaction to work, & the standard four dNTPs (A,G,C,T) can still be used. Nested PCRs cannot use the DUTP-UNG system, as the bases of a nested PCR is two back-to-back PCRs, where the amplicon from the first is used as the template for the second- using the DUTP-UNG system would degrade the first PCRs amplicon& leave no template for the second.

23
Q

Satellitism observed in cultures is most commonly associated with which of the following bacteria?

*Neisseria meningitidis

*Haemophilus influenzae

*Pasteurella canis

*Bordetella pertussis

A

The correct answer is Haemophilus influenzae
(which requires X factor & V factor) will grow in the hemolytic zone of Staphylococcus aureus on blood agar plates. Sheep blood agar plates (SAP) provide Hamophilus with X factor (hemin) & the hemolysis of RBCs by S. aureus releases V factor (NAD). The X &V factors (hemin & NAD, respectively) diffuse into the surrounding medium & promote the growth of Haemophilus in the area surrounding Staphylococcus colonies in a process called satellitism. For Haemophilus spp., the satellite test substitutes for the V factor test.

Neisseria meningitidis & Pasteurella canis do not have any special growth requirements. They are both able to grow independently on SAP & chocolate agar, but do not grow on MacConkey agar.

Bordetella pertussis requires special medium for isolation, but it isn’t able to obtain any of the required nutrients from the normal growth of other organisms in satellitism.

24
Q

Current CDC (2014) recommendations for initial HIV screening include FDA-approved immunoassay for detection of?

  • HIV-1p31 antigen

*HIV-1 & HIV-2 antibody, HIV-1 p24 antigen

*HIV-1 antibody & HIV-1 gp41 antigen

*HIV-1 & HIV-2 antibody

A

Fifth generation assays for HIV screening detect three markers: Hiv-1 & HIV-2 antibody, HIV-1 p24 antigen. Antigen detection identifies infection before antibody production occurs. Newer generation assays with sensitivity for HIV-1 p24 antigen can reduce the time between HIV infection and detection.
The Western blot has historically been used for the detection of HIV antibodies to antigens such as p24, p31, gp41, & gp 120/160. However, it is less sensitive than screening test & often demonstrates cross-reactivity. Despite this, it is till used for confirmatory HIV testing.

25
Which of the following is not a potential cause of allele dropout? *Mutations in the forward primer binding site *Mutations in the reverse primer binding site * Failed PCR * Poor quality template
Allele dropout occurs when one allele is disproportionately amplified over the other. If the PCR were to fail, there wouldn't be amplification of either allele. Therefore, Failed PCR is the correct answer. Mutations in the forward or reverse primer binding sites of one allele may lower the affinity of the template to the primers, thus decreasing the amplification of that allele. Starting with a poor-quality sample may also decrease the amplification of one allele.
26
What is the most commonly mutated oncogene seen in cancers? *TP53 *BRCA *KRAS *ATM
KRAS is the most commonly mutated oncogene seen in cancers. TP53 is seen in up to 50% of cancers, but it is a tumor suppressor gene, not oncogene. The remaining choices are found in high prevalence but only in certain types of cancers: BRCA is seen in breast & ovarian cancers, and ATM with ataxia telangiectasia.
27
The ratio of whole blood to anticoagulant is very important in the PT assay; at which hematocrit level should the standard anticoagulant be adjusted? * <50% *>70% *>55% *<35%
The effect of anticoagulant is too great to be ignored if the hematocrit value is greater than 55%, such as in cases of polycythemia. At this hematocrit concentration, the plasma volume is lower, and the excess citrate binds more calcium ions required for calcium-dependent clotting assays. This creates falsely prolonged clotting times affecting the PT & PTT test. The correction formula used to adjust the citrate to blood ratio is: Volume of Sodium Citrate = (1.85X10^-3)x(100- Pt HCT) x volume of whole blood drawn
28
How long should therapy continue for patients with hereditary hemochromatosis (HH)? * Therapy should continue throughout the lifetime * Therapy should continue only until ferritin levels have returned to normal * Therapy should continue for only one year * The length of therapy is variable for each patient
The regimen calls for weekly phlebotomy early in treatment to remove about 500mL of blood per treatment. Maintenance phlebotomist are required about every 3 months for life.
29
Which of the following Enterobacteriaceae produces Hydrogen Sulfide (H2S)? *Klebsiella species *Escherichia species *Salmonella species *Yersinia species
The correct answer is Salmonella. Salmonella (all serotypes) are facultative anaerobic, motile, Gram-negative rods commonly isolated from the intestines of humans & animals. Identification is primarily based on the ability of the organism to use citrate as the sole carbon source & lysine as nitrogen source in combination with H2S. Klebsiella species &Escherichia species will have yellow colonies on HE agar indicating no H2S production. Yersinia species will have salmon colonies on HE agar indicating no H2S production.
30
Which alpha thalassemia shows no anemia or evidence of disease, although a slight decrease in the MCV & MCHC may be seen? *Alpha thalassemia silent carrier *Alpha thalassemia minor *Alpha thalassemia intermedia ( Hemoglobin H disease) *Alpha thalassemia major (Hydrops fetalis)
The correct answer is Alpha thalassemia silent carrier, in this form there is no anemia manifested. However, clues, that this disorder may be present can be found by exhibiting a slight decrease in the MCV & MCHC. Alpha thalassemia minor patients typically have a mild anemia with a decrease in MCV & MCHC seen. Alpha thalassemia intermedia is the second most sever expression of the disease. Patients with Hemoglobin H disease exhibit a variable degree of microcytic, hypochromic anemia. patients may go into a hemolytic crisis during infection. Alpha thalassemia major, is the most sever expression of alpha thalassemia & is a lethal disease where infants die in utero or soon after birth.
31
The following characteristics are applicable to Interferon-Gamma Release Assays (IGRAs) EXCEPT: *Can be used in patients with active tuberculosis disease symptoms. *Preferable for patients who have received a bacillus Calmette-Guerin (BCG) vaccination. *Can be used instead of purified protein derivative (PPD) *Cannot differentiate latent TB from active tuberculosis infection.
The correct answer is that it can be used in patients with active TB disease symptoms. In addition, an IGRA method should not be used in children younger than 5yrs. IGRAs testing is preferable for patients who have received a BCG vaccination (either as a vaccine or for cancer therapy). Prior BCG vaccination does not cause false-positive IGRA test results. IGRAs can be used instead of purified protein derivative (PPD) skin test. It is recommended over TB skin testing in individuals 5yrs and older and who have low or moderate risk of disease progression. IGRAs cannot differentiate latent TB from active TB infection.
32
A patient is presenting with polydipsia, tiredness, & unexpected weight loss. Their A1C test comes back at 8%. Based on this, what HLA allele might you expect to see? *DR1 *DR2 *DR3 *A20
The patient's test results & symptoms are consistent with type 1 diabetes, which has been associated with HLA-DR3 allele. While HLA alleles are not diagnostic of any condition, strong correlations have been shown between having certain HLA alleles & disease.
33
A tech is working on a urine culture & finds the following isolates: Escherichia coli: >100,000 CFU/mL Enterococcus faecalis: 50,000 CFU/mL Klebsiella pneumoniae: 30,000CFU/mL How should the tech continue with the culture workup? *Quantitate culture & report as mixed urethral flora/contamination *Perform sensitivity on the E. coli & K. pneumoniae and list E. faecalis as a contamination *Perform sensitivity on the E. coli & list the others as contaminants *Reject culture due to contamination
The culture contains three organisms, all of which can be potential UT pathogens. One or two pathogens in culture will be identified, but three indicate contamination from the collection. All three pathogens are also showing significant quantities (>10,000 CFU/mL) and thus performing sensitivity on any of these can cause inappropriate treatment for the patient. Even though the E.coli is predominant ( colony count is greater than the others), the other organisms are in a significant quantity for workup & cannot be ignored in the assessment of contamination. E.faecalis is technically in a greater quantity than Klebsiella pneumonaie and can be urinary pathogen, so it should not be listed as a contaminant over the Klebsiella pneumoniae. Urine cultures are not rejected due to contamination, they are reported with quantity & possible contamination due to increased number of organisms. Rejection of specimens occurs prior to the culture set up for any inappropriate sources or incorrect handling or storage procedures that may have occurred.
34
Which of the following evaluation tools for documenting direct observations is the least subjective? *Anecdotal records *Checklist *Rating scale with detailed descriptions of traits *Rating scale with general descriptions of traits
A rating scale with detailed descriptions of traits is the least subjective evaluation tool for direct observations. While all four choices leave room for the common evaluation errors a detailed description of each trait eliminates some of the subjectivity in the evaluation process. An anecdotal record is a written description of the student's behavior written from the point of view of the evaluator, which is very subjective. The checklist is a list of statements describing the behaviors or tasks that the student must demonstrate & the evaluator decides if the student was successful or not. A rating scale with general descriptions of traits is a quick & easy form to fill out but it leaves too much room for subjectivity in the evaluation process.
35
Which of the following statements about diagnosing gestational diabetes is true? *Gestational diabetes is diagnosed with the same testing & criteria used for the diagnosis of diabetes for non-pregnant adults. *All non-diabetic pregnant women should be screened at 24-28 weeks of gestation. *Only diabetic pregnant women should be screened at 24-28 weeks gestation. *All pregnant women (diabetic or non-diabetic) should be screened at 24-28 weeks gestation.
The diagnostic testing used for diabetes during pregnancy is different than the diagnosis of diabetes for a non-pregnant adult. There are different screening test for gestational diabetes & an oral glucose tolerance test (OGTT) is used to confirm the diagnosis. All non-diabetic pregnant women should be screened at 24-28 weeks gestation. Screening is done using the 50 g OGTT. A plasma glucose= 140mg/mL (7.7 mmlo/L) at an hour after the glucose ingestion, indicates definitive testing is needed using 100g, 3-hour OGTT.
36
Mutations in which coagulation factor gene lead to prothrombin thrombophilia? *F1 *F2 *F3 *F5
The correct answer is F2. F2 is the coagulation factor gene that encodes for prothrombin. Mutations in this gene will lead to an excess production of prothrombin, which increases the risk of blood clots. F1 is fibrinogen, which can lead to an increased risk of bleeding or clotting, depending on whether too little or too much is produced. F3 is tissue factor, & F5 is proaccelerin, where decreases can also lead to bleeding, & altered protein can lead to Factor V Leiden.
37
A technologist put 5 tubes in a test tube rack and put 3mL of diluent in each tube. The tech then put 0.3 mL serum in the first tube and mixed it. Next, the tech then transferred 1 mL of the mixture from the first tube to the second tube. This process was carried on through tube number 5. What is the dilution factor in tube number 5? *200 *300 *2816 *4872
The cumulative dilution factor in any tube in a dilution series is determined by multiplying the dilution factors of all previous tubes in series, and the calculation also includes the tube in question. Therefore, dilution factor (in series) = tube #1's dilution factor X tube#2's dilution factor...X tube# n's dilution factor. The dilution in any individual tube can be determined by the simple formula: Dilution= sample volume/(sample volume+Diluent Volume). The dilution factor is the reciprocal of the dilution. In the first tube the individual dilution ratio would be 1:11. The individual ratios in each of the remaining four tubes is 1:4 in each one. However, the question asks for the cumulative dilution ratio in tube number 5. This can be easily determined by multiplying all the dilution factors together as follows: 11 X 4 X 4 X 4 X 4 = 2816 Thus the correct answer is 2816
38
A tech receives a call from the floor regarding antimicrobial therapy. The patient culture yielded an aerobic Gram-negative bacillus & the physician would like to use an antibiotic that inhibits cell wall synthesis. Which of the following antibiotics would be the best choice? *Gentamycin *Tetracycline *Ciprofloxacin *Cefazolin
The correct answer is Cefazolin. Cefazolin is part of the Cephalosporin family & part of the beta-lactam antibiotics with the Penicillins. Cephalosporin have a species range of both aerobic & anaerobic Gram-positive & Gram-negative species. The main target for these antibiotics are penicillin-binding proteins, which inhibit the cross-linking in peptidoglycan in the cell wall of the organism. This inhibition results in cell lysis and cell death.
39
A microbiology laboratory recently purchased a rapid identification instrument that uses a laser on the microorganisms, which produces an ion cloud. these ions are then separated in a tube & travel within the tube to a detector. The time of travel will be measured & a mass spectrum will be produced. Which of the following techniques uses this method? *API 20E *Viteck *Microscan *MALDI-TOF
MALDI-TOF is the correct answer because the name describes its methodology (Matrix-Assisted Laser Desorption Ionization Time of Flight mass spectrometry). With this methodology, an organism will be placed directly onto a plate & a chemical matrix will be applied. Afterwards, a laser will be applied to the sample & the matrix will absorb the energy creating an ion cloud.These ions will travel through a tube called a flight tube. The lighter ions will travel faster through the tube to the detector while the heavier ions will travel slower. The detector will measure the time of flight & report out a mass spectrum. This spectrum will be compared to other spectrums within the data library for identification.
40
The following organism is an anaerobic organism that produces spores & a double-zone of beta-hemolysis. *Pseudomonas aeruginosa *Clostridium perfringens *Enterobacter aerogenes *Cutibacterium (Propionibacterium) acnes
Clostridium perfringens is an anaerobic organism that is known to cause gas gangrene, food poisoning, & necrotizing enteritis. The identification of this organism begins with the appearance of a Gram-positive, spore- forming bacillus that produces a double-zone of beta-hemolysis on blood agar.
41
Which of the following best describes the direct antiglobulin (DAT) test principle? *AHG (anti-human globulin) detects antibody already sensitized to red cells. *AHG prevents antibody from sensitizing red cells. *AHG is directed against cell antigen.s *AHG is directed against plasma antibodies.
the correct answer is AHG detects antibody already sensitized to red cells. In the Direct Antiglobulin (DAT), AHG is added to patient cells after sufficient washing. This means that if a positive reaction occurs, the AHG is binding to the antibody (and/or complement proteins) already bound tot he patient RBC. Thus, it is a test to determine if in-vivo RBC sensitization has taken place. In-vivo antibody sensitization can take place during clinically significant events such as alloantibody formation& delayed transfusion reactions, autoimmune hemolytic anemia, HDFN, or drug-related mechanisms.
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Which of the following genes is not a oncogene? *TP53 *HER2 *ROS1 *RET
The correct answer is TP53. TP53 is a tumor suppressor gene, whose normal function is to stop cell division, but when mutated will allow for continual replication. HER2 is an oncogene associated with breast cancer, while ROS1 is seen in lung cancer, & RET in multiple endocrine neoplasia syndrome.
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A swab specimen from a wound culture is received in the lab. How should this specimen be processed for culture & Gram stain? *Roll swab back and forth on the slide, then inoculate the agar plates for culture. *Inoculate organism plates for culture, then roll the swab back and forth on the slide. *Rub swab back and forth across the slide, then inoculate agar plates for culture. *Inoculate agar plates for culture, then touch one area of the slide with the swab.
With a swab for culture & Gram stain, the culture plates should always be inoculated first to ensure that they do not become contaminated, and the slide set up last. When setting up a slide for Gram stain from a swab, it is important to roll the swab across the slide. This will ensure that the specimen is deposited evenly on the slide and maintain the integrity of the cell shape and morphology.
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MacConkey agar contains all of the following except: *Penicillin *Bile salts *Lactose *Crystal violet
The correct answer is Penicillin. MacConkey agar is a selective & differential medium. It selects for Enterobacteriaceae and other gram-negative bacilli using bile salts and crystal violet present in the medium, which inhibit gram-positive organisms. The medium is differential because it contains lactose, which will differentiate lactose fermenting gram-negative bacilli from non-lactose fermenting gram-negative bacilli. Lactose fermenters will appear pink on agar, and non-lactose fermenters will appear clear.
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All of the following are sites of active hematopoiesis in the adult EXCEPT: *Skull *Ribs *Liver *Pelvis
Except for the liver, each of the sites listed above are areas where hematopoiesis occurs in adults. The yolk sac, liver, & spleen are sites of hematopoiesis during fetal months.
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How should the production of a blue or purple color on the test pad of an Ictotest be interpreted? *Positive for bilirubin *Positive for ketones *Negative for bilirubin *Negative for ketones
The production of a blue or purple color on the test pad of an Ictotest be interpreted as positive for bilirubin.
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Which of the following combination of globin chains comprise Hemoglobin H? *Two alpha, two beta *Two alpha, two gamma *Four beta chains *Four alpha chains
The correct answer is 4 beta chains. Hemoglobin H is a tetramer made of 4 beta chains. Hemoglobin H occurs when there is very limited alpha chain availability used to make normal hemoglobin A. Hemoglobin h forms in those affected with alpha thalassemia major as well as in people with the combination of two-gene deletion alpha thalassemia and hemoglobin Constant Spring. 2 alpha, 2 betas is normal adult Hgb A 2 alpha, 2 gammas is fetal hemoglobin Hgb F 4 alpha chains cannot form a tetrad because they are highly insoluble & precipitate within the cell.
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Fetal lung maturity can be determined from amniotic fluid because the surfactant is PRIMARILY composed of: *Proteins *Cholesterol *Glycerol *Phosphatidylcholine and other phospholipids
Assessment of the status of amniotic fluid phospholipids has become important in determining fetal lung maturity. Pulmonary surfactant is a mixture of lipids, proteins, & glycoproteins & it is responsible for maintaining the surface tension of the alveoli preventing them from collapsing. As the fetal lungs mature, the phospholipid levels in the amniotic fluid increase, especially phosphatidylglycerol (PG) & phosphatidylcholine (lecithin). Another phospholipid, sphingomyelin has a constant amniotic concentration during pregnancy. It has been documented that the ratio of lecithin to sphingomyelin (L/S ratio), with respect to pediatric gestational age, is a reliable predictor of fetal lung maturity.
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